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J Med Chem ; 60(12): 5146-5161, 2017 06 22.
Article in English | MEDLINE | ID: mdl-28557445

ABSTRACT

The first-in-class soluble guanylate cyclase (sGC) stimulator riociguat was recently introduced as a novel treatment option for pulmonary hypertension. Despite its outstanding pharmacological profile, application of riociguat in other cardiovascular indications is limited by its short half-life, necessitating a three times daily dosing regimen. In our efforts to further optimize the compound class, we have uncovered interesting structure-activity relationships and were able to decrease oxidative metabolism significantly. These studies resulting in the discovery of once daily sGC stimulator vericiguat (compound 24, BAY 1021189), currently in phase 3 trials for chronic heart failure, are now reported.


Subject(s)
Heart Failure/drug therapy , Heterocyclic Compounds, 2-Ring/chemistry , Heterocyclic Compounds, 2-Ring/pharmacology , Pyrimidines/chemistry , Pyrimidines/pharmacology , Soluble Guanylyl Cyclase/metabolism , Structure-Activity Relationship , Administration, Intravenous , Administration, Oral , Animals , Blood Pressure/drug effects , Chemistry Techniques, Synthetic , Dogs , Hepatocytes/drug effects , Heterocyclic Compounds, 2-Ring/administration & dosage , Humans , Male , NG-Nitroarginine Methyl Ester/adverse effects , Pyrimidines/administration & dosage , Rats, Transgenic , Rats, Wistar , Soluble Guanylyl Cyclase/genetics
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